Nagai S, Izumi T
Chest Disease Research Institute, Kyoto University, Japan.
Curr Opin Pulm Med. 1996 Sep;2(5):419-23. doi: 10.1097/00063198-199609000-00012.
In 1955, Epler and Colby first described idiopathic bronchiolitis obliterans with organizing pneumonia. Davison and colleagues termed the entity cryptogenic organizing pneumonia. Clinically, the disease resembles a flu-like syndrome of acute or subacute onset. Other features include crackles, patchy infiltrates on chest radiograph, restrictive function, and decrease in diffusing capacity. Most cases of idiopathic bronchiolitis obliterans with organizing pneumonia (BOOP) respond dramatically to corticosteroids. However, some patients deteriorate rapidly. Differences between idiopathic or secondary BOOP and other interstitial lung diseases are vast. CT findings and bronchoalveolar lavage fluid lymphocytosis are helpful in differentiating BOOP from idiopathic pulmonary fibrosis.
1955年,埃普勒和科尔比首次描述了伴有机化性肺炎的特发性闭塞性细支气管炎。戴维森及其同事将该病症称为隐源性机化性肺炎。临床上,该病类似于急性或亚急性起病的流感样综合征。其他特征包括啰音、胸部X线片上的斑片状浸润、限制性肺功能以及弥散功能降低。大多数伴有机化性肺炎的特发性闭塞性细支气管炎(BOOP)病例对皮质类固醇有显著反应。然而,一些患者病情迅速恶化。特发性或继发性BOOP与其他间质性肺疾病之间的差异很大。CT表现和支气管肺泡灌洗液淋巴细胞增多有助于将BOOP与特发性肺纤维化区分开来。